ClinVar Miner

Submissions for variant NM_201525.4(ADGRG1):c.1236C>T (p.Val412=)

gnomAD frequency: 0.00001  dbSNP: rs768769972
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000894523 SCV001038509 benign not provided 2023-12-12 criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000894523 SCV001144080 likely benign not provided 2018-10-18 criteria provided, single submitter clinical testing
Natera, Inc. RCV001825801 SCV002089404 likely benign Bilateral frontoparietal polymicrogyria 2020-02-17 no assertion criteria provided clinical testing

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